Gradient elution isotachophoretic apparatus for separating, purifying, concentrating, quantifying, and/or extracting charged analytes and methods thereof

Patent metadata

Field	Value
Publication number	US-10067088-B2
Application number	US-201514746269-A
Country	US
Kind code	B2
Filing date	Jun 22, 2015
Priority date	Jun 20, 2014
Publication date	Sep 4, 2018
Grant date	Sep 4, 2018

Abstract

Gradient elution isotachophoretic apparatus, and systems for performing gradient elution isotachophoresis to separate, purify, concentrate, quantify, and/or extract charged analytes from a sample. The isotachophoretic apparatus include an electrophoretic assembly, a sampling assembly connected to the electrophoretic assembly, and/or a support structure connected to the electrophoretic assembly and/or to the sampling assembly. The system includes an isotachophoretic apparatus, and a controller communicatively coupled to the isotachophoretic apparatus. The controller includes a storage medium and a processor for executing computer readable and executable instructions.

First claim

What is claimed is:

1. An apparatus for performing gradient elution isotachophoresis (GEITP) to separate charged analytes in a sample, the apparatus comprising:
a moveable electrophoretic assembly comprising:
a separation unit,
a detection unit operably connected to the separation unit, wherein the detection unit comprises:
a detection unit support structure,
a conductivity detection device accommodated by the detection unit support structure,
a light source accommodated by the detection unit support structure, and
a light source detection device accommodated by the detection unit support structure, and

at least one moveable electrophoretic assembly support structure connected to at least one of the separation unit or the detection unit, wherein the at least one moveable electrophoretic assembly support structure is communicatively coupled to a motor, and wherein the at least one moveable electrophoretic assembly support structure and the motor are configured to provide movement of the moveable electrophoretic assembly in a Z direction or an X direction;

a sampling assembly operably connected to the moveable electrophoretic assembly; and
an apparatus support structure connected to at least one of the moveable electrophoretic assembly or the sampling assembly.

2. The apparatus of claim 1 , wherein the separation unit comprises:
at least one separation channel in a vertical orientation,
a leading electrolyte (LE) reservoir in open fluidic communication with the at least one separation channel,
a voltage supply device communicatively coupled to the at least one separation channel, and
a pressure control device connected to the LE reservoir.

3. The apparatus of claim 2 , wherein the separation unit includes a bundle of separation channels.

4. The apparatus of claim 1 , wherein:
the separation unit comprises at least one separation channel in a vertical orientation, and
the detection unit support structure provides an interface for alignment of the conductivity detection device, the light source, the light source detection device, and the at least one separation channel, such that in operation:
the conductivity detection device detects charged analytes present in the at least one separation channel,
the light source directs light through the at least one separation channel, exciting and emitting fluorescence in charged analytes contacted with sensor molecules and present therein, wherein the sensor molecules are capable of fluorescing upon contact with the charged analytes, and
the light source detection device detects the fluorescence emitted in the at least one separation channel.

5. The apparatus of claim 4 , wherein the detection unit support structure:
defines a separation channel cavity to accommodate the at least one separation channel therein,
defines a light source cavity to accommodate the light source therein, wherein the light source cavity is provided at a fluorescence excitation angle, and
defines a light source detection cavity to accommodate the light source detection device therein, wherein the light source detection cavity is provided at a fluorescence detection angle.

6. The apparatus of claim 5 , wherein:
the fluorescence excitation angle is from about 30° to about 150°, and
the fluorescence detection angle is from about 30° to about 150°.

7. The apparatus of claim 6 , wherein:
the fluorescence excitation angle is formed by intersection of an axis of the light source and a plane bisecting the separation channel cavity and parallel to a first side surface of the detection unit support structure, and the fluorescence detection angle is formed by intersection of an axis of the light source detection device and a plane which bisects the separation channel cavity and is parallel to a second side surface of the detection unit support structure.

8. The apparatus of claim 1 , wherein the at least one moveable electrophoretic assembly support structure comprises:
a first moveable support structure communicatively coupled to a first motor, wherein the first moveable support structure and the first motor are configured to provide movement of the moveable electrophoretic assembly in a Z direction,
a second moveable support structure communicatively coupled to a second motor, wherein the second moveable support structure and the second motor are configured to provide movement of the moveable electrophoretic assembly in an X direction, such that, in operation, the electrophoretic assembly is moveable in both the Z direction and the X direction.

9. The apparatus of claim 8 , wherein the first moveable support structure is connected to the second moveable support structure.

10. The apparatus of claim 1 , wherein the sampling assembly is moveable in a Y direction.

11. The apparatus of claim 1 , wherein:
the sampling assembly is connected to a sampling moveable support structure, and
the sampling moveable support structure is communicatively coupled to a motor, wherein the sampling moveable support structure and the motor are configured to provide movement of the sampling assembly in a Y direction.

12. The apparatus of claim 1 , wherein:
the at least one moveable electrophoretic assembly support structure comprises:
a first moveable support structure communicatively coupled to a first motor, wherein the first moveable support structure and the first motor are configured to provide translation of the moveable electrophoretic assembly in a Z direction, and
a second moveable support structure communicatively coupled to a second motor, wherein the second moveable support structure and the second motor are configured to provide translation of the moveable electrophoretic assembly in an X direction, and

the sampling assembly is connected to a third moveable support structure, wherein the third moveable support structure is communicatively coupled to a third motor, and wherein the third moveable support structure and the third motor are configured to provide translation of the sampling assembly in a Y direction.

13. The apparatus of claim 1 , wherein:
the separation unit comprises:
at least one separation channel in a vertical orientation,
a leading electrolyte (LE) reservoir in open fluidic communication with the at least one separation channel,
a voltage supply device communicatively coupled to the at least one separation channel, and
a pressure control device connected to the LE reservoir; and

the sampling assembly comprises a trailing electrolyte (TE) reservoir and a delivery reservoir.

14. The apparatus of claim 13 , wherein the TE reservoir comprises the sample and TE fluid, and wherein the apparatus further comprises a controller communicatively coupled to the moveable electrophoretic assembly and the sampling assembly, wherein the controller comprises a storage medium comprising computer readable and executable instructions and a processor for executing the computer readable and executable instructions wherein the processor executes the computer readable and executable instructions to:
(1) optionally pre-treat the at least one separation channel,
(2) insert LE fluid and sensor molecules capable of fluorescing upon contact with the charged analytes from the LE reservoir into the at least one separation channel,
(3) contact the at least one separation channel with the sample and TE fluid in the TE reservoir of the sampling assembly,
(4) separate the charged analytes via GEITP by:
(a) producing a pressure-driven counterflow of the LE fluid through the at least one separation channel with the pressure control device and/or the voltage supply device,
(b) applying a voltage

Assignees

• Henry Alyssa
• Konek Christopher
• Ross David
• Strychalski Elizabeth
• Applied Res Associates Inc
• The Us Secretary Of Commerce National Institute Of Standards And Technology

Inventors

• Henry Alyssa
• Konek Christopher
• Ross David
• Strychalski Elizabeth

Classifications

• C12N15/101 Primary

  by chromatography, e.g. electrophoresis, ion-exchange, reverse phase · CPC title

• G01N27/4473

  by electric means · CPC title

• G01N27/44743

  Introducing samples · CPC title

• G01N27/44721

  by optical means · CPC title

• G01N27/44769

  Continuous electrophoresis, i.e. the sample being continuously introduced, e.g. free flow electrophoresis [FFE] · CPC title